Leclercia adcarboxglata biocontrol strain efficiently inhibiting production of aflatoxins by aspergillus flavus and application thereof

ABSTRACT

The present invention relates to the microbiological field, and particularly relates to a leclercia adcarboxglata biocontrol strain efficiently inhibiting production of aflatoxins by Aspergillus flavus. The leclercia adcarboxglata biocontrol strain Wt16 was deposited at China Center for Type Culture Collection (CCTCC) on Jun. 13, 2017, and the accession number of the strain is CCTCC No. M2017331. The leclercia adcarboxglata strain Wt16 is isolated from peanut pods for the first time which can significantly inhibit aflatoxins production by Aspergillus flavus, and also has an extremely good effect on inhibiting aflatoxins production by aspergillus flavus for peanuts from different sources.

CROSS-REFERENCE TO RELATED APPLICATION

This application claims the benefit of China application serial No.201711228608.X, filed on Nov. 29, 2017. The entirety of theabove-mentioned patent application is hereby incorporated by referenceherein and made a part of this specification.

FIELD

The present invention belongs to the microbiological field, andparticularly relates to a leclercia adcarboxglata biocontrol strainefficiently inhibiting production of aflatoxins by Aspergillus flavusand an application thereof.

BACKGROUND

Aspergillus flavus is a pathogenic fungus capable of producing powerfulcarcinogenic and highly toxic mycotoxins aflatoxins. Aflatoxins includefamilies B, G and M, wherein B1 is the most common and most toxic. Theaflatoxins can pollute grain crops such as peanuts and corn extensively,seriously threatening the health of human and livestock, and causing ahuge economic loss. Therefore, it is urgent to strengthen prevention andcontrol of aspergillus flavus and toxin pollution.

Currently, there are three methods of prevention and control ofAspergillus flavus, namely, physical, chemical and biological controlmethods. However, chemical control is expensive and is likely to causeenvironmental pollution. In addition, while chemical control is adoptedfor controlling pathogenic bacteria, the pathogenic bacteria are proneto drug tolerance and even drug resistance to chemical agents. Physicalcontrol is time-consuming and labour-intensive, and its toxin-removingrate is not high, and it easily causes nutrient loss. Biological controlhas advantages of being safe, efficient and durable. Therefore, it is ofgreat significance to strengthen the research on the biologicalprevention and control of aspergillus flavus for China's agriculturalindustry and economic benefits.

The leclercia adcarboxglata is rarely isolated from environmental andclinical specimens. According to current reports, the leclerciaadcarboxglata is generally isolated from blood, wound secretions,gallbladder tissues, a peritoneal dialysis solution, and urine.Moreover, reports have not been seen in the existing research regardinguse of leclercia adcarboxglata for inhibiting production of aflatoxinsby aspergillus flavus.

SUMMARY OF THE INVENTION

The present invention provides a leclercia adcarboxglata biocontrolstrain which can efficiently inhibit production of aflatoxins byAspergillus flavus and an application thereof. In an embodiment, theleclercia adcarboxglata biocontrol strain Wt16 is provided, which wasdeposited at China Center for Type Culture Collection (CCTCC) on Jun.13, 2017. The deposition address is Wuhan University, Wuhan, China, andthe accession number of the strain is CCTCC No. M2017331.

According to the present invention, the leclercia adcarboxglata straincapable of inhibiting aflatoxins production by Aspergillus flavus wasisolated from peanut pods for the first time. A screening methodcomprises the following steps: washing the peanut pods picked from apeanut field in Huangpi of Hubei Province with tap water, placing thewashed peanut pods in an LB solid medium for culture, picking growingbacteria with an inoculating loop, transferring the picked bacteria to afresh LB solid medium for plate streaking, picking a single colony aftertransferring for several times, and performing co-culture tests on thepicked single colony and aspergillus flavus in a medium (namelyperforming co-culture antibacterial tests by in vitro inoculation ofpeanuts with the aspergillus flavus) to measure toxin productivity; andfinally screening a leclercia adcarboxglata biocontrol strain Wt16capable of remarkably inhibiting aspergillus flavus from generatingtoxins. The strain was deposited at China Center for Type CultureCollection (CCTCC) with an accession number of CCTCC No. M2017331.

The strain is identified with a 16S rDNA specific amplificationtechnique, morphological characteristics, and physiological andbiochemical tests. The results show that the strain is a leclerciaadcarboxglata strain belonging to enterobacteriaceae, and is also aunique strain of leclercia adcarboxglata genus. The 16S rRNA sequence ofthe leclercia adcarboxglata biocontrol strain Wt16 is as shown in SEQ IDNO.1.

TABLE 1 Major biological characteristics of leclercia adcarboxglataWt16: Gram Nutrient Culture Culture V.P M.R Cellulose Nitrate stainingOxygen Spore Capsule requirements temperature time test test Oxidasedegradation reduction Negative Facultative No No Low 25-37° C. 12-24 hNegative Negative Negative Negative Positive anaerobic

In an embodiment, an inhibitor for aflatoxins production by Aspergillusflavus is provided which comprises biologically pure culture of theleclercia adcarboxglata biocontrol strain Wt16.

In an embodiment, the inhibitor is in a form of a liquid, a dust, a drywettable powder or a dry wettable granule.

In an embodiment, the inhibitor is in a form of a liquid and theleclercia adcarboxglata biocontrol strain Wt16 is present at aconcentration of (1-9)×10⁷ CFU/mL.

In an embodiment, the inhibitor is a fermentation liquid of theleclercia adcarboxglata biocontrol strain Wt16. A preparation method ofthe fermentation liquid comprises the following steps: activating theleclercia adcarboxglata strain Wt16 in an LB plate, performing culturingin an incubator at 25-37° C. for 24 h, picking a single colony ofleclercia adcarboxglata with a teasing needle, transferring the singlecolony to a liquid medium for shaking culture for 12-24 h, sucking 1-3%of a culture solution, and transferring the culture solution to a freshliquid medium for shaking culture for 12-24 h, so as to obtain theantagonistic leclercia adcarboxglata strain Wt16 fermentation liquid.

In an embodiment, a method of preparing the inhibitor is provided, themethod comprising:

-   -   activating the leclercia adcarboxglata strain Wt16 in an LB        plate,    -   performing culturing in an incubator at 25-37° C. for 24 h,    -   picking a single colony of leclercia adcarboxglata with a        teasing needle,    -   transferring the single colony to a liquid medium for shaking        culture for 12-24 h,    -   sucking 1-3% of a culture solution, and    -   transferring the culture solution to a fresh liquid medium for        shaking culture for 12-24 h, so as to obtain an antagonistic        leclercia adcarboxglata strain Wt16 fermentation liquid.

In an embodiment, an application of the inhibitor for inhibiting theproduction of aflatoxins by Aspergillus flavus is provided. The specificmethod is as follows: coating surfaces of a biological sample with theinhibitor or mixing the inhibitor with a biological sample to inhibitthe production of aflatoxins by Aspergillus flavus, so as to prevent thebiological sample from aflatoxin pollution.

In an embodiment, an application of the leclercia adcarboxglata strainWt16 for inhibiting the production of aflatoxins by Aspergillus flavusis provided. The specific method is as follows: coating surfaces of abiological sample with a fermentation liquid of the leclerciaadcarboxglata strain Wt16 or mixing a fermentation liquid of theleclercia adcarboxglata strain Wt16 with the biological sample toinhibit the production of aflatoxins by Aspergillus flavus, so as toprevent the biological sample from aflatoxin pollution.

The leclercia adcarboxglata strain Wt16 which has a good effect oncontrolling aspergillus flavus is isolated from peanut pods for thefirst time. The strain can significantly inhibit aflatoxins productionby Aspergillus flavus, and also has an extremely good effect oninhibiting aflatoxins production by aspergillus flavus for peanuts fromdifferent sources.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows growth conditions of the inoculated peanut powder inembodiment 2. The left picture shows the growth condition of the peanutpowder inoculated with the aspergillus flavus and then cultured for 9days by using a Sabourand liquid medium as a control; and the rightpicture shows the growth condition of the peanut powder inoculatedsimultaneously with the leclercia adcarboxglata strain Wt16 and theaspergillus flavus and then cultured for 9 days.

FIG. 2 shows growth conditions of the peanut kernels before and afterinoculation in embodiment 3. The left picture shows the growth conditionof the peanuts inoculated simultaneously with the leclerciaadcarboxglata strain Wt16 and the aspergillus flavus and then culturedfor 9 days; and the right picture shows the growth condition of thepeanuts inoculated with aspergillus flavus and then cultured for 9 daysby using a Sabourand liquid medium as a control.

DETAILED DESCRIPTION

The method comprises the following steps: washing peanut pods pickedfrom a peanut field in Huangpi of Hubei Province with tap water, placingthe washed peanut pods in an LB solid medium for culture, pickinggrowing bacteria with an inoculating loop, transferring the pickedbacteria to a fresh LB solid medium for plate streaking, picking asingle colony after transferring for several times, and performingco-culture tests on the picked single colony and aspergillus flavus in amedium to measure toxin productivity, namely performing co-cultureantibacterial tests by in vitro inoculation of peanuts with theaspergillus flavus; and finally screening a leclercia adcarboxglatabiocontrol strain Wt16 capable of remarkably inhibiting the productionof aflatoxins by Aspergillus flavus. The strain was deposited at ChinaCenter for Type Culture Collection (CCTCC) with an accession number ofCCTCC No. M2017331.

Embodiment 1

1) activating the leclercia adcarboxglata strain Wt16 in an LB plate,performing culturing in an incubator at 37° C. for 24 h, picking asingle colony of leclercia adcarboxglata with a teasing needle,transferring the single colony to a triangular flask with 15 mL of LBliquid medium, and performing shaking culture at 28° C. and at 200r·min⁻¹ for 12 h; and sucking 1% of a culture solution, transferring theculture solution to a triangular flask with 15 mL of LB liquid medium,and performing shaking culture at 28° C. and at 200 r·min⁻¹ for 12 h, soas to obtain an antagonistic strain fermentation liquid;

2) culturing the leclercia adcarboxglata fermentation liquid (finalconcentration is 1×10⁷ CFU/mL) and thriving aspergillus flavussuspension after 7 days of culture (final spore concentration is 5.0×10⁵spores mL⁻¹) together in a Sabourand liquid medium at 28° C. and at 200rpm for 5 days, wherein each treatment is repeated for 3 times; and

3) measuring the content of aflatoxin B1 in the culture solution (Table2).

TABLE 2 Control effect of biocontrol bacteria on aspergillus flavusTreatment A. flavus A. flavus + CCTCC No. M 2017331 Content of AFB1215.22 ± 36.59 0.8167 ± 0.09518 (ng/ml)

As can be seen from the test result, the leclercia adcarboxglata strainCCTCC No. M2017331 has an aflatoxin inhibiting rate of 99.6%, showingthat the strain has the capacity of inhibiting aflatoxin production.

Embodiment 2

1) grinding “Zhonghua No. 6” peanut kernels taken from a peanut field ofHubei Province into powder, weighing and placing 1 g of the peanutpowder to a culture dish, and at the same time adding 1 mL ofaspergillus flavus spore suspension (5×10⁵/mL) and 1 mL of CCTCCM2017331 bacterial liquid (1×10⁷ CFU/mL). A Sabourand medium is used forreplacing the CCTCC M2017331 fermentation liquid as a control;

2) culturing the inoculated peanut powder in an incubator at 28° C. for9 days, observing the growth condition (FIG. 1), then adding 15 mL of70% aqueous methanol to obtain a mixture, and placing the mixture into ashaker for 30 min after being mixed in a vortex manner; taking 3 mL ofsupernatant, adding 8 mL of ultrapure water and performing vortexcentrifugation;

3) taking 8 mL of supernatant, and measuring the content of aflatoxin B1(Table 3) by an immunoaffinity column-HPLC method. 3 repeats are set inthe test. The left picture of FIG. 1 shows the growth condition of thepeanut powder inoculated with the aspergillus flavus and then culturedfor 9 days by using a Sabourand liquid medium as a control; and theright picture shows the growth condition of the peanut powder inoculatedsimultaneously with the leclercia adcarboxglata strain Wt16 and theaspergillus flavus and then cultured for 9 days.

TABLE 3 Control effect of biocontrol bacteria on peanut aspergillusflavus Treatment A. flavus A. flavus + CCTCC No. M 2017331 Content ofToxins 516.61 ± 51.91 86.84 ± 14.13 (ng/ml)

As can be seen from the test result, the strain CCTCC M2017331 on the“Zhonghua No. 6” peanuts has an aflatoxin inhibiting rate ofapproximately 83%, showing that the strain has a good effect ofcontrolling aflatoxins during the storage of peanuts.

Embodiment 3

1) taking 10 “Luhua No. 8” peanut kernels from a peanut field of AnhuiProvince, coating the surfaces of the peanut kernels with thefermentation liquid of the leclercia adcarboxglata strain Wt16 and atthe same time adding 1 mL of aspergillus flavus spore suspension(5×10⁵/mL). A Sabourand medium is used for replacing the CCTCC M2017331fermentation liquid as a control;

2) culturing the inoculated peanut kernels in an incubator at 28° C. for9 days, observing the growth condition (FIG. 2), then grinding thepeanut kernels into peanut powder, adding 15 mL of 70% aqueous methanol,and placing the mixture into a shaker for 30 min after being mixed in avortex manner; and taking 3 mL of supernatant, adding 8 mL of ultrapurewater, and performing vortex centrifugation. The left picture of FIG. 2shows growth condition of the peanuts inoculated simultaneously with theleclercia adcarboxglata strain Wt16 and the aspergillus flavus and thencultured for 9 days; and the right picture shows the growth condition ofthe peanuts inoculated with aspergillus flavus and then cultured for 9days by using a Sabourand liquid medium as a control;

3) taking 8 mL of supernatant, and measuring the content of aflatoxin B1(Table 4) by an immunoaffinity column-HPLC method. 3 repeats are set inthe test.

TABLE 4 Control effect of biocontrol bacteria on peanut aspergillusflavus Treatment A. flavus A. flavus + CCTCC No. M 2017331 Content ofToxins 449.95 ± 42.51 51.74 ± 3.30 (ng/ml)

As can be seen from the test result, the strain CCTCC M2017331 on the“Luhua No. 8” peanuts has a rate of inhibiting the aspergillus flavusfrom producing toxins being approximately 88.5%, showing that the strainhas an extremely good biocontrol effect on peanuts of different kinds.

What is claimed is:
 1. A leclercia adcarboxglata biocontrol strain Wt16,wherein the leclercia adcarboxglata biocontrol strain Wt16 was depositedat China Center for Type Culture Collection (CCTCC) on Jun. 13, 2017,and the accession number of the strain is CCTCC No. M2017331.
 2. Aninhibitor for aflatoxins production by Aspergillus flavus, comprising aman-made culture of a leclercia adcarboxglata biocontrol strain Wt16deposited at China Center for Type Culture Collection (CCTCC) on Jun.13, 2017 with the access number CCTCC No. M2017331.
 3. The inhibitor ofclaim 2, wherein the inhibitor is in a form of a liquid, a dust, a drywettable powder or a dry wettable granule.
 4. The inhibitor of claim 2,wherein the inhibitor is in the form of a liquid and the leclerciaadcarboxglata biocontrol strain Wt16 is present at a concentration of(1-9)×10⁷ CFU/mL.
 5. The inhibitor of claim 2, wherein the inhibitor isan fermentation liquid of the leclercia adcarboxglata biocontrol strainWt16, a preparation method of the fermentation liquid includesactivating the leclercia adcarboxglata strain Wt16 in an LB plate,performing culturing in an incubator at 25-37° C. for 24 h, picking asingle colony of leclercia adcarboxglata with a teasing needle,transferring the single colony to a liquid medium for shaking culturefor 12-24 h, sucking 1-3% of a culture solution, and transferring theculture solution to a fresh liquid medium for shaking culture for 12-24h, so as to obtain an antagonistic leclercia adcarboxglata strain Wt16fermentation liquid.
 6. A method of inhibiting production of aflatoxinsby Aspergillus flavus, comprising: coating surfaces of a biologicalsample with the inhibitor of claim 2 or mixing the inhibitor of claim 2with a biological sample to inhibit the production of aflatoxins byAspergillus flavus.
 7. A method of preparing the inhibitor of claim 2,comprising: activating the leclercia adcarboxglata strain Wt16 in an LBplate, performing culturing in an incubator at 25-37° C. for 24 h,picking a single colony of leclercia adcarboxglata with a teasingneedle, transferring the single colony to a liquid medium for shakingculture for 12-24 h, sucking 1-3% of a culture solution, andtransferring the culture solution to a fresh liquid medium for shakingculture for 12-24 h, so as to obtain an antagonistic leclerciaadcarboxglata strain Wt16 fermentation liquid.